Suppliers / Zhejiang Golden-Shell Pharmaceutical

Zhejiang Golden-Shell Pharmaceutical

China Updated 9 July 2026

Zhejiang Golden-Shell Pharmaceutical is an API manufacturer based in China. It holds 4 active US drug master files across a filed portfolio of 3 molecules.

4
active US DMFs
0
valid CEPs
0
registered plants
0
filings across 0 regulators

What they file, and where

Molecule Regulators Docs
Glucosamine US FDA 2
Chitosan Low Molecular Weight (20-200 Mpa.S) US FDA 1
N-Acetylglucosamine US FDA 1

Also appears on these molecule pages

Glucosamine API

Questions about Zhejiang Golden-Shell Pharmaceutical

Does Zhejiang Golden-Shell Pharmaceutical hold a US DMF or a CEP?
Zhejiang Golden-Shell Pharmaceutical holds 4 active US drug master files. A drug master file is a submission to the FDA describing how an ingredient is made; a CEP is the EDQM's certificate that the substance meets its European Pharmacopoeia monograph. Both are filings rather than approvals.
What does Zhejiang Golden-Shell Pharmaceutical make?
3 molecules are on record against Zhejiang Golden-Shell Pharmaceutical, including Glucosamine, Chitosan Low Molecular Weight (20-200 Mpa.S) and N-Acetylglucosamine. Each links through to that molecule's full manufacturer list.

Answered from this company's own record. Where a register holds nothing, the question is not asked rather than answered with a zero. How we count our figures.

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Comparable suppliers

Zhejiang Cheng Yi Pharmaceutical shares 1 molecule Meck Pharmaceuticals And Chemicals shares 1 molecule Zhejiang Fengrun Biotech shares 1 molecule Zhejiang Zhoushan Putuo Xinxing Pharmas shares 1 molecule

Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability